Structural origins of morphing in plant tissues

Plant tissues are able to generate complex movements via shape modifications. These effects are tightly related to distinctive multi-scale composite architectures of the plant material, and can therefore largely be interpreted by composite mechanics principles. Here, we propose a generic framework for the analysis and prediction of the shape morphing of intricate biological composite materials, arising from changes in humidity. We have examined in depth the hierarchical structures of three types of seed pods for which we propose a theoretical scheme that is able to accurately simulate the relevant shape deformations. The validity and generality of this approach are confirmed by means of laboratory scale synthetic models with similar architectures leading to equivalent morphing patterns. Such synthetic configurations could pave the way to future morphing architectures of advanced materials and structures.

[1]  Ellad B. Tadmor,et al.  Surface effects in non-uniform nanobeams: Continuum vs. atomistic modeling , 2010 .

[2]  Peter Fratzl,et al.  Tensile and compressive stresses in tracheids are induced by swelling based on geometrical constraints of the wood cell , 2007, Planta.

[3]  E. Altus,et al.  Stochastic surface effects in nanobeam sensors , 2010 .

[4]  H. Abramovich,et al.  The electromechanical response of multilayered piezoelectric structures , 2004, Journal of Microelectromechanical Systems.

[5]  J. Dumais,et al.  “Vegetable Dynamicks”: The Role of Water in Plant Movements , 2012 .

[6]  Haiyi Liang,et al.  Growth, geometry, and mechanics of a blooming lily , 2011, Proceedings of the National Academy of Sciences.

[7]  R. Elbaum,et al.  Insights into the microstructures of hygroscopic movement in plant seed dispersal. , 2014, Plant science : an international journal of experimental plant biology.

[8]  L. Mahadevan,et al.  Hygromorphs: from pine cones to biomimetic bilayers , 2009, Journal of The Royal Society Interface.

[9]  R. Kupferman,et al.  Geometry and Mechanics in the Opening of Chiral Seed Pods , 2011, Science.

[10]  Janet Braam,et al.  In touch: plant responses to mechanical stimuli. , 2004, The New phytologist.

[11]  L. Mahadevan,et al.  How the Cucumber Tendril Coils and Overwinds , 2012, Science.

[12]  C. Dawson,et al.  How pine cones open , 1997, Nature.

[13]  K. Schulgasser,et al.  The hierarchy of chirality. , 2004, Journal of theoretical biology.

[14]  E. Gamstedt,et al.  Modelling of effects of ultrastructural morphology on the hygroelastic properties of wood fibres , 2007 .

[15]  L. Ionov Biomimetic Hydrogel‐Based Actuating Systems , 2013 .

[16]  John L. Harper,et al.  The Shapes and Sizes of Seeds , 1970 .

[17]  L. Mahadevan,et al.  How the Venus flytrap snaps , 2005, Nature.

[18]  Peter Fratzl,et al.  Plants control the properties and actuation of their organs through the orientation of cellulose fibrils in their cell walls. , 2009, Integrative and comparative biology.

[19]  R. Elbaum,et al.  The Role of Wheat Awns in the Seed Dispersal Unit , 2007, Science.

[20]  Doron Shilo,et al.  Ferromagnetic shape memory flapper for remotely actuated propulsion systems , 2013 .

[21]  André R Studart,et al.  Self-shaping composites with programmable bioinspired microstructures , 2013, Nature Communications.

[22]  V. T. Forsyth,et al.  Nanostructure of cellulose microfibrils in spruce wood , 2011, Proceedings of the National Academy of Sciences.